United States · FDA National Drug Code directory
Fexofenadine hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 10202-229_d5914c05-e8db-4c79-82d0-a279d1304118
- Product NDC
- 10202-229
- Form
- TABLET, FILM COATED
- Composition / generic term
- Fexofenadine hydrochloride
- Labeler
- 7-eleven
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150115
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 10202-229-66
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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